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Journal of Anatomy and Histopathology

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Effect of Silicon Dioxide Nanoparticles on Liver Morphology of Rats in Parenteral Administration

https://doi.org/10.18499/2225-7357-2021-10-4-85-88

Abstract

The issue of the potential safety of silicon dioxide nanoparticles (SDNPs) remains relevant. In this connection, in order to use the unique capabilities of silicon nanostructures for biomedical purposes, as well as to level their toxic effects, a detailed study of these nanoparticles interaction with cells and tissues in vivo is required.

The aim of the research is to reveal morphofunctional changes in a rat's liver after a single parenteral administration of 12 nm silicon dioxide nanoparticles for the period of six months.

Material and methods. Using general histological and immunohistochemical methods to study the rats' liver after a single parenteral administration of 1 ml of silicon dioxide nanoparticles at a dose of 7 mg/kg of body weight at a concentration of 2 mg/ml. The sections of the rats' liver were studied by general histological and immunohistochemical methods after injection of 1mL of a SDNPs saline suspension at a concentration of 2 mg/mL (7mg/kg of body weight). Control animals were injected with 1 ml of saline solution. The material was collected in 21 days, 2, 4 and 6 months months after the administration of the SDNPs and it was fixed in 10% neutral formaldehyde.

Results. The formation of granulomas in the liver on the 21st day of the experiment and an increase in the number of Kupfer cells were revealed. However, by the 2nd month of the experiment, the number of granulomas significantly decreases compared to the 21st day of the experiment and continues to decrease in subsequent periods. The average size of granulomas decreases during the 2nd month of the experiment and does not change during the subsequent periods of the experiment. After 6 months of the experiment, the morphofunctional state of the liver is characterized by slightly pronounced aseptic inflammation.

Conclusion. A single parenteral administration of silicon dioxide nanoparticles causes pronounced aseptic inflammation of the liver, decreasing by the 6th month of the experiment. Connective tissue remodeling in the liver is not observed at all periods of the experiment.

About the Authors

G. Yu. Yukina
First Pavlov State Medical University of St.-Petersburg
Russian Federation

 Galina Yukina

 ul. L'va Tolstogo, 6-8, St-Petersburg, 197022 



E. G. Sukhorukova
First Pavlov State Medical University of St.-Petersburg
Russian Federation

 ul. L'va Tolstogo, 6-8, St-Petersburg, 197022 



I. V. Polovnikov
First Pavlov State Medical University of St.-Petersburg
Russian Federation

 ul. L'va Tolstogo, 6-8, St-Petersburg, 197022 



E. A. Kryzhanovskaya
First Pavlov State Medical University of St.-Petersburg
Russian Federation

 ul. L'va Tolstogo, 6-8, St-Petersburg, 197022 



References

1. Zaitseva NV, Zemlyanova MA, Zvezdin VN, Dovbysh AA, Gmoshinskiy IV, Khotimchenko SA. Impact of silica dioxide nanoparticles on the morphology of internal organs in rats by oral supplementation. Health Risk Analysis. 2016 Apr;(4):80–94] (in Russian). doi: 10.21668/health.risk/2016.4.10

2. Podkolodnaya OA, Ignatieva EV, Podkolodnyi NL, Kolchanov NA. Pathways for penetration of nanoparticles into mammalian organisms, their biocompatibility and cellular effects. Uspekhi Sovremennoi Biologii. 2012;132(1):3–15] (in Russian).

3. Sutunkova MP, Solovyeva SN, Katsnelson BA, Gurvich VB, Privalova LI, Minigalieva IA, et al. Some peculiarities of the organism’s responses to a long-term inhalation of silica-containing submicron (predominantly, nanoscale) particles in a real industrial aerosol. Toxicological Review. 2017 Jun 28;(3):17–26] (in Russian). doi: 10.36946/0869-7922-2017-3-17-26

4. Yukina GYu, Zhuravskii SG, Panevin AA, Galagudza MM, Tomson VV, Blum NM. Macrophage granulomas and mast cells as beginning organ remodeling in case of silicon dioxide nanoparticles chronic toxicity. Translational medicine. 2016;3(2):70–9] (in Russian).

5. Ebbesen M, Jensen TG. Nanomedicine: Techniques, Potentials, and Ethical Implications. Journal of Biomedicine and Biotechnology. 2006;1:1–11. doi: 10.1155/jbb/2006/51516

6. Eom H-J, Choi J. Oxidative stress of silica nanoparticles in human bronchial epithelial cell, Beas-2B. Toxicology in Vitro. 2009 Oct;23(7):1326–32. doi: 10.1016/j.tiv.2009.07.010

7. Lu X, Tian Y, Zhao Q, Jin T, Xiao S, Fan X. Integrated metabonomics analysis of the size-response relationship of silica nanoparticles-induced toxicity in mice. Nanotechnology. 2010 Dec 23;22(5):055101. doi: 10.1088/0957-4484/22/5/055101

8. Nabeshi H, Yoshikawa T, Matsuyama K, Nakazato Y, Tochigi S, Kondoh S, et al. Amorphous nanosilica induce endocytosis-dependent ROS generation and DNA damage in human keratinocytes. Particle and Fibre Toxicology. 2011 Jan 15;8(1):1–10. doi: 10.1186/1743-8977-8-1

9. Napierska D, Thomassen LCJ, Rabolli V, Lison D, Gonzalez L, Kirsch-Volders M, et al. SizeDependent Cytotoxicity of Monodisperse Silica Nanoparticles in Human Endothelial Cells. Small. 2009 Apr 6;5(7):846–53. doi: 10.1002/smll.200800461

10. Park MVDZ, Annema W, Salvati A, Lesniak A, Elsaesser A, Barnes C, et al. In vitro developmental toxicity test detects inhibition of stem cell differentiation by silica nanoparticles. Toxicology and Applied Pharmacology. 2009 Oct;240(1):108–16. doi: 10.1016/j.taap.2009.07.019

11. Thomassen LCJ, Aerts A, Rabolli V, Lison D, Gonzalez L, Kirsch-Volders M, et al. Synthesis and Characterization of Stable Monodisperse Silica Nanoparticle Sols for in Vitro Cytotoxicity Testing. Langmuir. 2009 Aug 21;26(1):328–35. doi:10.1021/la902050k

12. Ye Y, Liu J, Xu J, Sun L, Chen M, Lan M. NanoSiO2 induces apoptosis via activation of p53 and Bax mediated by oxidative stress in human hepatic cell line. Toxicology in Vitro. 2010 Apr;24(3):751–8. doi: 10.1016/j.tiv.2010.01.001


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For citations:


Yukina G.Yu., Sukhorukova E.G., Polovnikov I.V., Kryzhanovskaya E.A. Effect of Silicon Dioxide Nanoparticles on Liver Morphology of Rats in Parenteral Administration. Journal of Anatomy and Histopathology. 2021;10(4):85-88. (In Russ.) https://doi.org/10.18499/2225-7357-2021-10-4-85-88

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ISSN 2225-7357 (Print)